Clearance Summary
LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES received FDA 510(k) clearance under submission number K002445, sponsored by Medtronic Physio-Control Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-01-31.
- Submission: K002445
- Applicant / Sponsor: Medtronic Physio-Control Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2001-01-31
Classification & Regulation
This clearance is catalogued under FDA product code MKJ and 21 CFR 870.5310, within the Cardiovascular review panel as a Class III device.